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阿糖胞苷用于成人急性淋巴细胞白血病的诱导、挽救及巩固治疗。

Cytosine arabinoside for induction, salvage, and consolidation therapy of adult acute lymphoblastic leukemia.

作者信息

Stryckmans P, De Witte T, Bitar N, Marie J P, Suciu S, Solbu G, Debusscher L, Bury J, Peetermans M, Andrien J M

出版信息

Semin Oncol. 1987 Jun;14(2 Suppl 1):67-72.

PMID:3296209
Abstract

During A-ALL induction treatment, HD-ara-C (2.5 g/m2 IV, day 1), does not produce any beneficial effect, whereas the hematologic toxicity is increased. A 3-month consolidation phase comprising intermittent MTX, ara-C and 6-TG is not significantly affecting either DFI or survival in A-ALL. The association of HD-ara-C and m-AMSA appears to be a promising salvage therapy for the 20% A-ALL refractory to first induction therapy. The quality of autologous bone marrow graft, harvested after HD-ara-C, seems to be impaired as suggested by a delayed recovery of PMN and platelets. HD-ara-C (3 g/m2 X N) given the days before cyclophosphamide and TBI as conditioning treatment for BMT does not seem to induce prohibitory additional toxicity. Whether HD-ara-C was given four to six times or eight to 12 times gave no significant difference in early toxicity.

摘要

在急性淋巴细胞白血病(A-ALL)诱导治疗期间,大剂量阿糖胞苷(HD-ara-C,2.5 g/m²静脉注射,第1天)未产生任何有益效果,反而血液学毒性增加。为期3个月的巩固期,包括间歇性甲氨蝶呤(MTX)、阿糖胞苷和6-硫鸟嘌呤(6-TG),对A-ALL的无病生存期(DFI)或生存率均无显著影响。大剂量阿糖胞苷与米托蒽醌联合使用,对于20%对首次诱导治疗无效的A-ALL患者而言,似乎是一种有前景的挽救疗法。如中性粒细胞(PMN)和血小板恢复延迟所示,在大剂量阿糖胞苷治疗后采集的自体骨髓移植质量似乎受损。在环磷酰胺和全身照射(TBI)前几天给予大剂量阿糖胞苷(3 g/m²×N)作为骨髓移植(BMT)的预处理,似乎不会引发额外的严重毒性。大剂量阿糖胞苷给药4至6次或8至12次,早期毒性无显著差异。

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